Ann Surg Treat Res.  2014 Jul;87(1):9-13. 10.4174/astr.2014.87.1.9.

Multicenter nonrandomized trial of ramosetron versus palonosetron in controlling chemotherapy-induced nausea and vomiting for colorectal cancer

Affiliations
  • 1Department of Surgery, Chungnam National University School of Medicine, Daejeon, Korea.
  • 2Department of Surgery, Chungbuk National University School of Medicine, Cheongju, Korea.
  • 3Department of Surgery, Dankook University College of Medicine, Cheonan, Korea.
  • 4Department of Surgery, Eulji University School of Medicine, Daejeon, Korea.
  • 5Department of Surgery, Konyang University College of Medicine, Daejeon, Korea.
  • 6Department of Surgery, Sooncheonhyang University College of Medicine, Cheonan, Korea. ssurge@sch.ac.kr

Abstract

PURPOSE
Chemotherapy-induced nausea and vomiting (CINV) have a negative impact on patients' quality of life and frequently pointed to as a major factor for treatment abandonment. Serotonin (5-HT3) receptor antagonist is considered as key treatment for CINV. Ramosetron and palonosetron are recently developed 5-HT3 receptor antagonists and known as more superior than other first-generation 5-HT3 receptor antagonists. The purpose of this study was to compare the efficacy of ramosetron and palonosetron and determine which drug is more effective for prevention of CINV.
METHODS
Colorectal cancer patients treated with chemotherapy were enrolled consecutively. Patients were assigned to receive intravenous injection of ramosetron 0.3 mg or palonosetron 0.25 mg at 30 minutes before initiation of moderately emetogenic chemotherapy. Ramosetron group added oral administration of 0.1 mg ramosetron on the second and third days of chemotherapy. Efficacy parameter consisted of nausea and vomiting.
RESULTS
Ninety-one patients received ramosetron and 89 patients received palonosetron. Presentation of vomiting and nausea symptoms was not significantly different between the two groups during acute (0-24 hours) and delayed period (after 24 hours).
CONCLUSION
The incidence of CINV between the ramosetron and the palonosetron group has not shown any difference during acute, delayed, and overall period.

Keyword

Vomiting; Ramosetron; Palonosetron; Adjuvant chemotherapy; Colorectal neoplasms

MeSH Terms

Administration, Oral
Chemotherapy, Adjuvant
Colorectal Neoplasms*
Drug Therapy
Humans
Incidence
Injections, Intravenous
Nausea*
Quality of Life
Receptors, Serotonin, 5-HT3
Serotonin
Vomiting*
Receptors, Serotonin, 5-HT3
Serotonin

Figure

  • Fig. 1 Proportion of patients with no emetic episodes during the acute, delayed and overall time period (n = 180). CINV, chemotherapy-induced nausea and vomiting.


Cited by  1 articles

Ramosetron versus Palonosetron in Combination with Aprepitant and Dexamethasone for the Control of Highly-Emetogenic Chemotherapy-Induced Nausea and Vomiting
Jin Hyoung Kang, Jung Hye Kwon, Yun-Gyoo Lee, Keon Uk Park, Ho Jung An, Joohyuk Sohn, Young Mi Seol, Hyunwoo Lee, Hwan-Jung Yun, Jin Seok Ahn, Ji Hyun Yang, Hunho Song, Dong-Hoe Koo, Jin Young Kim, Gun Min Kim, Hwa Jung Kim
Cancer Res Treat. 2020;52(3):907-916.    doi: 10.4143/crt.2019.713.


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